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NCT Number: NCT05066412

Prophylactic CD45RA-depleted DLI After Haploidentical Transplantation/RIC

To assess safety of prophylactic escaladed dose of T naïve depleted (CD45RA depleted donor lymphocyte infusion, in patients with malignant hemopathie who received an allogeneic stem cell transplant from an haplo-identical donor, after a reduced intensity conditionning regiment.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

HUG

Geneva, Canton of Geneva, 1205, Switzerland

Location status: Recruiting

Location contact

Anne-Claire Mamez

CONTACT

[email protected]

+41795534996

About this study

Primary Objective is to determine whether the administration of prophylactic CD45RAneg (CD45RAneg) memory/effector T lymphocytes is feasible and safe in the early post-transplant period for patients with haploidentical transplant and RIC conditioning.

Donor lymphocytes are isolated from the original donor by non-mobilized mononuclear cell leukapheresis. Repetitive intravenous infusions (up to 3) of escalating doses of CD45RAneg cells, prepared from the leukapheresis by CliniMACS® technology (CD45RA-depletion), storage in vapor nitrogen.

Escalating doses of CD45RAneg cells, for patients with haploidentical graft, intervals of 6-8 weeks, if GvHD is absent starting ≥ 4 weeks from the day of transplantation.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients who received a stem cell graft from a haploidentical donor after RIC for hematologic malignancies
  • Written informed consent of patient and donor obtained

Exclusion criteria

  • Participant taking Prednisone (or equivalent steroid)
  • Participant taking Prednisone (or equivalent steroid)
  • Participant taking Mycophenolate Mofetil
  • Participant taking Cyclosporine/tacrolimus at therapeutic blood levels
  • Progressive hematologic malignancy before transplant
  • Second allogeneic transplant
  • Acute GvHD ≥ grade 2
  • Chronic moderate or severe GvHD (NIH consensus criteria)
  • Hematologic or molecular relapse of the primary malignancy requiring chemotherapy or unmanipulated DLI (receiving prophylactic antileukemic agent, eg TKI, is not an exclusion criteria)
  • Donor aberrant CD45RA expression due to a polymorphism in CD45 gene
  • Participation in another interventional clinical trial within 30 days prior to inclusion
  • Pregnant or nursing women. Sexually active women with childbearing potential as well as sexually active male patients who are unwilling to use an effective method of contraception during participation in the study from time of inclusion until 2 months after last dose of CD45RAneg DLI infusion
  • Inability to follow the procedures of the study, including, but not limited to, language problems, psychological disorders, dementia

Treatment and study plan

CD45RAneg cells, prepared from mononuclear cell leukapheresis by CliniMACS® technology

Other

CD45RAneg cells, prepared from mononuclear cell leukapheresis by CliniMACS® technology

Primary outcomes

  1. acute transfusion reaction (CTCAE ≥ 2)

    Time frame: 24 hours after each CD45RA neg DLI infusion

    acute transfusion reaction after each DLI infusion (CTCAE ≥ 2)

  2. acute GvHD grade II-IV

    Time frame: within 8 weeks after each CD45RAneg DLI infusion

    acute GvHD grade II-IV measured with MAGIC score

Study contacts

Contact information is provided by the study sponsor or research team.

Anne-Claire Mamez

CONTACT

[email protected]

+41786656487

Sponsors and collaborators

Lead sponsor

University Hospital, Geneva

Other

Registry information

Official study title

A Phase I Clinical Trial Assessing Prophylactic Donor CD45RA-depleted Lymphocyte Infusions Into Patients Transplanted with Stem Cell Grafts from Haploidentical Donors After Reduced Intensity Conditioning

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Oct 4, 2021
Registry last updated
Feb 13, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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